EU Medical Device Technical Files Workshop
Wednesday 12 June 2019 @ 10:30 am - 4:00 pm
SEHTA, Psephos Biomedica & Mosaic Surgical would like to invite you to attend our EU Medical Device Technical Files Workshop.
The new EU Medical Device Regulation (MDR) is in its implementation phase and will be effective from May 2020. All medical devices will need to comply with this new legislation. Similarly, the IVD Regulation (IVDR) will be in force from May 2022. Many companies are not yet ready for the journey let alone have a roadmap of how to get to compliance.
This one-day event will:
Provide you with an overview of the key requirements for technical documentation in order to comply with the MDR and your conformity assessment
Assist you in assessing your company’s current preparedness for the transition
Provide a clear, practical guide to the next steps that you and your company need to take to meet Technical documentation requirements to gain CE Marking under the MDR
Costs to attend: – You will be invoiced separately after registration
SEHTA Members: £240+ VAT per delegate
SEHTA non-members :£280+ VAT per delegate (it’s free to join SEHTA – Please click here)
Special Offer if you book 2 workshops in advance
£430 + VAT SEHTA Members / £510 + VAT SEHTA non-members per delegate
Series 2 workshop is on Software/AI Medical Device CE Marking on 24 April
For full details and to book your place, please click here.